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Journal Abstract Search

227 related items for PubMed ID: 1865235

  • 1. Limb-girdle syndrome: a genetic study of 22 large Brazilian families. Comparison with X-linked Duchenne and Becker dystrophies.
    Passos-Bueno MR, Vainzof M, Pavanello Rde C, Pavanello-Filho I, Lima MA, Zatz M.
    J Neurol Sci; 1991 May; 103(1):65-75. PubMed ID: 1865235
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  • 3. Is dystrophin always altered in Becker muscular dystrophy patients?
    Vainzof M, Passos-Bueno MR, Pavanello RC, Zatz M.
    J Neurol Sci; 1995 Jul; 131(1):99-104. PubMed ID: 7561956
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  • 4. Serum creatine-kinase (CK) and pyruvate-kinase (PK) activities in Duchenne (DMD) as compared with Becker (BMD) muscular dystrophy.
    Zatz M, Rapaport D, Vainzof M, Passos-Bueno MR, Bortolini ER, Pavanello Rde C, Peres CA.
    J Neurol Sci; 1991 Apr; 102(2):190-6. PubMed ID: 2072118
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  • 5. Serum CK-MB activity in progressive muscular dystrophy: is it of nosologic value?
    Vainzof M, Zatz M, Otto PA.
    Am J Med Genet; 1985 Sep; 22(1):81-7. PubMed ID: 4050853
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  • 6. Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G.
    Passos-Bueno MR, Vainzof M, Moreira ES, Zatz M.
    Am J Med Genet; 1999 Feb 19; 82(5):392-8. PubMed ID: 10069710
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  • 8. Improved diagnosis of Becker muscular dystrophy by dystrophin testing.
    Hoffman EP, Kunkel LM, Angelini C, Clarke A, Johnson M, Harris JB.
    Neurology; 1989 Aug 19; 39(8):1011-7. PubMed ID: 2668783
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  • 10. Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families.
    Passos-Bueno MR, Moreira ES, Marie SK, Bashir R, Vasquez L, Love DR, Vainzof M, Iughetti P, Oliveira JR, Bakker E, Strachan T, Bushby K, Zatz M.
    J Med Genet; 1996 Feb 19; 33(2):97-102. PubMed ID: 8929943
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  • 11. A survey of manifesting carriers of Duchenne and Becker muscular dystrophy in Wales.
    Norman A, Harper P.
    Clin Genet; 1989 Jul 19; 36(1):31-7. PubMed ID: 2766561
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  • 12. A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy.
    Bueno MR, Moreira ES, Vainzof M, Chamberlain J, Marie SK, Pereira L, Akiyama J, Roberds SL, Campbell KP, Zatz M.
    Hum Mol Genet; 1995 Jul 19; 4(7):1163-7. PubMed ID: 8528203
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  • 13. Distinction of Becker from limb-girdle muscular dystrophy by means of dystrophin cDNA probes.
    Norman A, Thomas N, Coakley J, Harper P.
    Lancet; 1989 Mar 04; 1(8636):466-8. PubMed ID: 2563842
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  • 15. Estimate of the intrafamilial correlation for serum creatine kinase and pyruvate kinase in females at risk for Duchenne and Becker muscular dystrophies.
    Rabbi-Bortolini E, Dal Colletto GM, Passos-Bueno MR, Vainzof M, Rapaport D, Zatz M.
    Hum Hered; 1991 Mar 04; 41(6):370-8. PubMed ID: 1797630
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  • 17. Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 3. Differential diagnosis and prognosis.
    Nicholson LV, Johnson MA, Bushby KM, Gardner-Medwin D, Curtis A, Ginjaar IB, den Dunnen JT, Welch JL, Butler TJ, Bakker E.
    J Med Genet; 1993 Sep 04; 30(9):745-51. PubMed ID: 8411069
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  • 19. Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequence.
    Passos-Bueno MR, Terwilliger J, Ott J, Vainzof M, Love DR, Davies KE, Zatz M.
    Am J Med Genet; 1991 Jan 04; 38(1):140-6. PubMed ID: 2012126
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